RS869312971 RORB

Health Risk Chr 9:74634755
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Epilepsy
idiopathic generalized
susceptibility to
15
Inborn genetic diseases
Epilepsy
idiopathic generalized
susceptibility to
15
Other Variants in RORB
rs869312972 rs1563959514 rs766539793 rs1587393982 rs1587401875 rs1824167579 rs763192623 rs1824250656 rs1824166369 rs2118532750
Ask Dr. Hemsworth about this variant